A Physical Activity Program for Female Nursing Home Residents at Risk of Osteoporosis
Primary Purpose
Osteoporosis
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Physical activity and education intervention
Education intervention
Sponsored by
About this trial
This is an interventional prevention trial for Osteoporosis focused on measuring Osteoporosis, Chinese women, nursing home, physical activity, RCT
Eligibility Criteria
Inclusion Criteria (cluster level-nursing home):
- have at least 100 female residents aged 60 to 75 years
Exclusion Criteria (cluster level-nursing home):
- are participating in any other clinical trials
Inclusion Criteria (participant level):
- female
- aged 60 to 75 years
Exclusion Criteria (participant level):
- have a previous diagnosis of osteoporosis
- are osteoporotic
- are taking medicines that would affect calcium or bone metabolism
- are already physically active (i.e. exercise at least three times a week at a moderate or higher intensity for ≥ 30 min)
- have taken part in any physical activity program within the past year
- sustain any medical condition that would put them at risk by taking part in moderate intensity exercises
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Physical activity and education intervention
Education intervention
Arm Description
Outcomes
Primary Outcome Measures
Change of habitual physical activity
The primary outcome is the change of habitual physical activity from baseline to 12 months, which will be measured using the International Physical Activity Questionnaire - Short Form (IPAQ-SF).
Secondary Outcome Measures
Incidental falls
A fall is defined as "an event which results in a person coming to rest in advertently on the ground or floor or other lower level".
Change in bone mineral density (BMD)
BMD (g/cm2) of lumbar spine (L1-L4) and proximal femoral neck
Full Information
NCT ID
NCT04168658
First Posted
November 16, 2019
Last Updated
November 16, 2019
Sponsor
Chengdu Jinjiang Maternity and Child Health Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04168658
Brief Title
A Physical Activity Program for Female Nursing Home Residents at Risk of Osteoporosis
Official Title
A Pilot and Feasibility Cluster Randomized Controlled Trial of Physical Activity Program for Female Nursing Home Residents at Risk of Osteoporosis
Study Type
Interventional
2. Study Status
Record Verification Date
November 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 10, 2020 (Anticipated)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
June 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chengdu Jinjiang Maternity and Child Health Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Worldwide, osteoporosis causes more than 8.9 million fractures per annum. Osteoporosis used to be a significant public health concern that most commonly affected Caucasian women in Northern Europe and the United States. Recently, it has become a major public health problem in Asia, most notably among Chinese women.
We intend to conduct a cluster randomized controlled trial (RCT) to examine if a physical activity and education intervention, compared with an education-only intervention (waiting list for physical activity), can result in improved physical activity, reduced falls, and maintaining bone mass, among female nursing home residents in China. The aim of the current pilot and feasibility trial is to test the feasibility and acceptability of conducting these interventions.
A pilot and feasibility cluster RCT will be conducted for females aged 60 to 75 years living in nursing homes in Chengdu, the capital of Sichuan Province, Western China. The unit of cluster randomization is the nursing home. A total of four nursing homes (two state-owned and two private-owned) will be involved in the pilot and feasibility trial. They will be randomly selected and afterwards randomly assigned to either the intervention group (2 nursing homes) or control group (2 nursing homes). We seek to recruit 20 women from each nursing home.
The intervention group participants will exercise with the research staff or under supervision of the trained nursing home staff, and will receive face-to-face workshops, booklet, newsletters, phone calls, and short message service (SMS) reminders. Participants in the control group will only receive educational materials (i.e. face-to-face workshops and booklet) and will be wait listed to receive no other interventions of this study until after the post-intervention. All participants will be referred to doctors for advice and standard care as usual.
The primary outcome is the change of habitual physical activity from baseline to 12 months, which will be measured using the International Physical Activity Questionnaire - Short Form (IPAQ-SF). Secondary outcomes include incidental falls and change in bone mineral density (BMD) from baseline to 12 months. The study results will serve to provide an estimate of the effect size, intraclass correlation coefficient (ICC) and rates of eligibility, recruitment and attrition, which may enable a more accurate sample size calculation for a definitive RCT.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
Osteoporosis, Chinese women, nursing home, physical activity, RCT
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Physical activity and education intervention
Arm Type
Experimental
Arm Title
Education intervention
Arm Type
Active Comparator
Intervention Type
Combination Product
Intervention Name(s)
Physical activity and education intervention
Intervention Description
At least six staff from each nursing home that assigned to the intervention group will be invited to attend two educational workshops. Participants in the intervention group will receive the following interventions.
Face-to-face workshops: Five 1-hour educational workshops on physical activity will be delivered in months 1, 3, 5, 7 and 9 of the program held at each nursing home.
Booklet: At the first educational workshop, each participant will be provided with a pictorial booklet.
Exercise: The physical activity training consists of 50-60 min exercise sessions three times a week on non-consecutive days for 12 months.
Others (newsletters, phone calls, and reminders): The intervention group will also receive newsletters containing myth dispelling information on osteoporosis and physical activity, motivational phone calls and a total of 52 SMS via mobile phones (reminders to attend workshop sessions and physical activity motivating messages) over 12 months.
Intervention Type
Behavioral
Intervention Name(s)
Education intervention
Intervention Description
Participants in the control group will only receive educational materials (i.e. face-to-face workshops and booklet) and will be wait listed to receive no other interventions of this study until after the post-intervention.
Primary Outcome Measure Information:
Title
Change of habitual physical activity
Description
The primary outcome is the change of habitual physical activity from baseline to 12 months, which will be measured using the International Physical Activity Questionnaire - Short Form (IPAQ-SF).
Time Frame
Baseline to 12 months post-baseline
Secondary Outcome Measure Information:
Title
Incidental falls
Description
A fall is defined as "an event which results in a person coming to rest in advertently on the ground or floor or other lower level".
Time Frame
12 months starting from the baseline
Title
Change in bone mineral density (BMD)
Description
BMD (g/cm2) of lumbar spine (L1-L4) and proximal femoral neck
Time Frame
Baseline to 12 months post-baseline
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria (cluster level-nursing home):
have at least 100 female residents aged 60 to 75 years
Exclusion Criteria (cluster level-nursing home):
are participating in any other clinical trials
Inclusion Criteria (participant level):
female
aged 60 to 75 years
Exclusion Criteria (participant level):
have a previous diagnosis of osteoporosis
are osteoporotic
are taking medicines that would affect calcium or bone metabolism
are already physically active (i.e. exercise at least three times a week at a moderate or higher intensity for ≥ 30 min)
have taken part in any physical activity program within the past year
sustain any medical condition that would put them at risk by taking part in moderate intensity exercises
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Li Tang, PhD
Phone
+8615002872018
Email
tangli207@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Li Tang, PhD
Organizational Affiliation
Chengdu Jinjiang Maternity and Child Health Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
A Physical Activity Program for Female Nursing Home Residents at Risk of Osteoporosis
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